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U.S. Department of Health and Human Services

510(k) Premarket Notification
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11 to 20 of 23 Results
ProductCode: DQY Applicant: CORDIS CORP. Decision Date To: 11/30/2021
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Export all 23 Records to ExcelExport to Excel | Download Files | More About 510(k)
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510(K)
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cordis slalom pta balloon catheter CORDIS CORP. K003159 10/30/2000
cordis shuttle catheter w/ sideholes CORDIS CORP. K921311 09/09/1992
cordis shuttle catheter CORDIS CORP. K915777 02/11/1992
cordis m3 pta dilatation catheter CORDIS CORP. K003920 06/15/2001
cordis introducer guide CORDIS CORP. K001136 04/28/2000
cordis envoy & vista brite tip guiding catheters CORDIS CORP. K962362 08/08/1996
cordis ducor ptr system CORDIS CORP. K811971 08/13/1981
cordis brite tip, envoy guiding catheter CORDIS CORP. K952185 08/02/1995
cordis 9 f guiding catheter CORDIS CORP. K925131 05/06/1993
cordis 7 french 0.072 i.d. ptca guiding catheter CORDIS CORP. K912777 09/20/1991
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